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Dl-PHPB inhibits platelet aggregation and affects the balance of PGI2/TXA2 and fibrinolytic system of rats / 中国药学杂志
Chinese Pharmaceutical Journal ; (24): 1021-1025, 2015.
Article in Zh | WPRIM | ID: wpr-859520
Responsible library: WPRO
ABSTRACT

OBJECTIVE:

To investigate the effect of potassiam 2-(1-hydroxypentyl)-benzoae (dl/-PHPB) on platelet aggregation, the balance of PGI2/TXA, and fibrinolytic system of rats.

METHODS:

Rats were randomly divided into 5 groups; control group, low (1.3 mg·kg-1), middle (3.9 mg·kg-1) and high (12.9 mg·kg-1) dose of dl-PHPB groups and ticlopidine group. Blood was taken from the abdominal aorta 30 min after dl-PHPB administrated intravenously, and the rate of platelet aggregation was detected by platelet aggregometer. The expression of CD62p on the surface of platelet was determined by flow cytometry. The contents of 6-Keto-PGF1α, thromboxane B2 (TXB2), t-PA and PAT-1 in serum were measured by radio-immuno assay and FLISA kit, respectively.

RESULTS:

dl-PHPB inhibited rat platelet aggregation induced by A DP in dose-dependent manner more potently compared with AA, collagen and thrombin. dl-PHPB also decreased the expression of CD62p. It increased the level of 6-keto-PGF1α, the metabolite of prostaglandin I2 (PGL2) and reduced the content of PAI-1. But dl/-PHPB had no effect on the contents of TXB2 the metabolite of TXA2 and t-PA.

CONCLUSION:

dl-PHPB may significantly inhibit rat platelet aggregation induced by ADP, increase the ratio of PG12/TXA2 and enhance the activity of fibrinolytic system.
Key words
Full text: 1 Index: WPRIM Language: Zh Journal: Chinese Pharmaceutical Journal Year: 2015 Type: Article
Full text: 1 Index: WPRIM Language: Zh Journal: Chinese Pharmaceutical Journal Year: 2015 Type: Article